O[C@H]1C[C@@H]2C(NC(=O)C3=C(O)C4=C(OCO4)C=C23)[C@H](O)[C@@H]1O

InChIKey=SBTGHBALOCEVOR-ZXHOVYBOSA-N

C14H15NO7

309.274

Organic compounds

Alkaloids and derivatives

Amaryllidaceae alkaloids

Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids

Not available

Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids

Phenanthridines and derivatives Isoquinolones and derivatives Tetrahydroisoquinolines Benzodioxoles 1-hydroxy-4-unsubstituted benzenoids Cyclitols and derivatives Vinylogous acids Secondary carboxylic acid amides Secondary alcohols Lactams Polyols Acetals Azacyclic compounds Oxacyclic compounds Organopnictogen compounds Hydrocarbon derivatives Organonitrogen compounds Organic oxides

Aromatic heteropolycyclic compounds

Phenanthridone-type amaryllidaceae alkaloid - Benzoquinoline - Phenanthridine - Isoquinolone - Quinoline - Tetrahydroisoquinoline - Benzodioxole - 1-hydroxy-4-unsubstituted benzenoid - Cyclitol or derivatives - Benzenoid - Vinylogous acid - Cyclic alcohol - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Lactam - Oxacycle - Azacycle - Organoheterocyclic compound - Acetal - Polyol - Carboxylic acid derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Alcohol - Organopnictogen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as phenanthridine- and phenanthridone-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids compounds based on the phenanthridine or the phenanthridone skeleton. Phenanthridone-type alkaloids have the highest oxygenated C ring in all Amaryllidaceae alkaloids, and they always show an amide group in ring B. On the contrary, alkaloids of the phenanthridine type often show completely aromatic ring system, occasionally with a methylation quaternary nitrogen atom.

Not available